183612-76-2

Upstream product

• 153683-14-8 2-(2-Bromo-5-methoxyphenyl)-1-iodoethane 
• 25226-97-5 3-methoxyphenethyl iodide 
• 5020-41-7 2-(3-methoxyphenyl)-ethanol 

Downstream Products

• 183612-81-9 (6aS,9aS)-2-Methoxy-6a,7,10,11-tetrahydro-6H-benzo[4,5]indeno[1,7a-c]pyrrole-8-carboxylic acid 4-nitro-phenyl ester 
• 183612-78-4 C₂₃H₂₅NO₃ 
• 183612-79-5 (6aS,9aS)-8-Benzyl-2-methoxy-6a,7,8,9,10,11-hexahydro-benzo[4,5]indeno[1,7a-c]pyrrol-6-one 
• 183612-80-8 8-benzyl-2-methoxy-6a,7,8,9,10,11-hexahydro-6H-benzo[4,5]indeno[1,7a-c]pyrrole 
• 183612-77-3 (3S,5aR,8aS,8bR)-7-Benzyl-5a-[2-(2-bromo-5-methoxy-phenyl)-ethyl]-3-isopropyl-8b-methyl-octahydro-pyrrolo[3',4':3,4]pyrrolo[2,1-b]oxazol-5-one 

Relevant academic research and scientific papers

An asymmetric route to the conanine BCDE ring system. A formal total synthesis of (+)-conessine

The first enantioselective synthesis of the known (+)-conessine precursor (+)-benzohydrindan 23 from the chiral nonracemic bicyclic lactam 1 is described. The key transformation was the highly diastereoselective (3 + 2) cycloaddition of azomethine ylide 1